Clinical Research Track
Submitting WG/Project/Implementer Group
Clinical Interoperability Council
Clinical Research Studies currently require direct redundant entry of clinical data that should reside in EHR systems that conform to meaningful use. As data is managed in a pharmaceutical sponsor environment, the CRF data is updated, and may vary from the original source that presented by the EHR. This leads to difficulties for regulatory inspectors and reviewers in tracing back clinical data to source data, as well as redundant duplication of effort by site personnel, and general quality issues. Given the extreme cost and extended time required for randomized clinical trials, it would be substantially better to utilize EHR source data in clinical databases more efficiently.
Proposed Track Lead
Transcelerate BioPharma, Inc. EDC Vendors TBD
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